39552-81-3

基本信息
對(duì)氨基苯乙酸甲酯
4-氨基苯乙酸甲酯
2-(4-氨基苯基)乙酸甲酯
甲基-(4-氨基苯基)乙酸酯,98%
METHYL P-AMINOPHENYLACETATE
Methyl 4-aminobenzeneacetate
METHYL-(4-AMINOPHENYL)ACETATE
p-(Methoxycarbonylmethyl)aniline
4-Aminophenylacetic acid methyl ester
Benzeneacetic acid, 4-amino-, methyl ester
1-(CHLOROMETHYL)-3,5-BIS(METHYLSULFONYL)BENZENE
1-(CHLOROMETHYL)-3,5-BIS(METHYLSULPHONYL)BENZENE
4-Aminophenylacetic acid methyl ester, 4-[(Methoxycarbonyl)methyl]aniline
物理化學(xué)性質(zhì)
制備方法

67-56-1

1197-55-3

39552-81-3
中間體8a:2-(4-氨基苯基)乙酸甲酯的合成 將4-氨基苯乙酸(10.0 g,66.6 mmol)溶解于甲醇(350 mL)中,攪拌并濃縮。緩慢滴加濃硫酸(3.88 mL,72.77 mmol)。將反應(yīng)混合物在50℃下攪拌反應(yīng)過夜,隨后冷卻至室溫并進(jìn)行真空濃縮。將濃縮后的混合物用水稀釋,用碳酸鈉(Na2CO3)中和至固體析出,然后用二氯甲烷(DCM)進(jìn)行萃取。有機(jī)層用無水硫酸鈉(Na2SO4)干燥,過濾后濃縮,得到2-(4-氨基苯基)乙酸甲酯(9.75 g,59.02 mmol,收率89%)。 方法2:RT:0.60 min,m/z 165.9 [M + H]+。
參考文獻(xiàn):
[1] Patent: US2014/303218, 2014, A1. Location in patent: Paragraph 0088-0089
[2] Dalton Transactions, 2018, vol. 47, # 15, p. 5259 - 5268
[3] Patent: WO2016/51193, 2016, A1. Location in patent: Paragraph 00249; 00250; 00251
[4] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 6, p. 1784 - 1789
[5] Journal of Medicinal Chemistry, 1997, vol. 40, # 7, p. 1049 - 1062